Videos
Walkthroughs and explainers for medical device compliance — pricing, audit prep, technical documentation, and more.
11:05
eQMS MCP Server: Talk to Your QMS! (OpenRegulatory Formwork)
Dr. Oliver Eidel
7:50
AI-Generate Your QMS + Technical Documentation in 3 Minutes
Dr. Oliver Eidel
43:32
Free ISO 19011 Internal Auditor Training (for Medical Devices)
Dr. Oliver Eidel
12:04
Free MDR PRRC Course (Person Responsible for Regulatory Compliance)
Dr. Oliver Eidel
9:40
Medizinprodukteberater Course: Examples
Dr. Oliver Eidel
10:40
Medizinprodukteberater Course: Requirements, Tasks, Responsibilities
Dr. Oliver Eidel
6:23
Post-Market Surveillance: The Periodic Safety Update Report (PSUR)
Dr. Oliver Eidel
12:34
Medical Device Post-Market Surveillance: The Plan
Dr. Oliver Eidel
5:16
Medical Device Post-Market Surveillance: The Process
Dr. Oliver Eidel
6:15
Free Medical Device Post-Market Surveillance Course: Concepts
Dr. Oliver Eidel
7:52
Post Market Clinical Follow-up: The Report (Medical Device Clinical Evaluation)
Dr. Oliver Eidel
9:28
Post-Market Clinical Follow-up: Concepts and Plan
Dr. Oliver Eidel
6:19
Clinical Evaluation: Post-Market Surveillance (PMS) Database Search
Dr. Oliver Eidel
11:52
Literature Search For Clinical Evaluation of Medical Devices
Dr. Oliver Eidel
12:37
Clinical Evaluation: The Clinical Evaluation Report (CER)
Dr. Oliver Eidel
6:24
Clinical Evaluation: Understanding the Phases and the Plan
Dr. Oliver Eidel
5:18
Free Clinical Evaluation Course, Part 1: Understanding the Process
Dr. Oliver Eidel
15:16
Registering Your UDI in EUDAMED (Medical Device Database)
Dr. Oliver Eidel
5:00
Creating a UDI-PI and Data Matrix Code at IFA
Dr. Oliver Eidel
2:29
Generating the Basic UDI-DI at IFA
Dr. Oliver Eidel
5:24
Hack: UDI-DI for Free with HPC at IFA (for Medical Devices)
Dr. Oliver Eidel
7:10
IFA: Ordering a PPN via Auftragstabelle B3
Dr. Oliver Eidel
9:05
Registering As a Customer at IFA to Create a UDI
Dr. Oliver Eidel
7:22
Creating a Medical Device UDI at IFA (Unique Device Identifier)
Dr. Oliver Eidel
10:36
UDI-PI and Barcode With Application Identifiers in GS1
Dr. Oliver Eidel
3:13
Creating the Basic UDI-DI as GMN in GS1
Dr. Oliver Eidel
10:15
How to Use The GS1 GTIN Manager (UDIs for Medical Devices)
Dr. Oliver Eidel
11:00
Registering a UDI with GS1 (Unique Device Identifiers for Medical Devices)
Dr. Oliver Eidel
11:59
Free Course: Understanding Unique Device Identifiers (UDIs) For Medical Devices
Dr. Oliver Eidel
6:55
Software Validation (ISO 13485 QMS), Part 2
Dr. Oliver Eidel
8:06
Software Validation (as part of your QMS, for the ISO 13485)
Dr. Oliver Eidel
6:07
Purchasing: Supplier Checklist For ISO 13485 Compliance
Dr. Oliver Eidel
10:39
Purchasing SOP For Medical Devices (ISO 13485)
Dr. Oliver Eidel
16:05
Human Resources Administration For Medical Device Companies (ISO 13485)
Dr. Oliver Eidel
12:18
Vigilance For EU MDR and ISO 13485 Compliance
Dr. Oliver Eidel
13:11
CAPAs (Corrective and Preventive Actions) For ISO 13485 Compliance
Dr. Oliver Eidel
14:05
EU MDR Post-Market Surveillance, Part 2 (+ ISO 13485)
Dr. Oliver Eidel
9:27
EU MDR Post-Market Surveillance, Part 1 (+ ISO 13485)
Sven Piechottka
8:45
Feedback Management For Medical Device (ISO 13485) Compliance
Sven Piechottka
6:35
Internal Audits (ISO 13485 Compliance)
Sven Piechottka